ライフサイエンスコーパス: Mus spretus

1 s musculus subspecies, and a sister species, Mus spretus.

2 he genomes of Rattus norvegicus (brown rat), Mus spretus (Algerian mouse), and Apodemus sylvaticus (w

3 elomeres is different from that observed for Mus spretus and human telomeres.

4 rosatellite scan together with outcrosses to Mus spretus and M. castaneous followed by a subsequent t

5 g mouse evolution, in the common ancestor of Mus spretus and Mus domesticus.

6 k contrast, CDK3 from two wild-mice species (Mus spretus and Mus mus castaneus) lack this mutation.

7 tribution of IAPE elements in the genomes of Mus spretus and Mus musculus inbred strains and wild-cau

8 /6 J, 129S1/SvImJ and CAST/EiJ) and species (Mus spretus and Mus pahari).

9 l contact mapping in wild-derived SPRET/EiJ (Mus spretus) and laboratory inbred C57BL/6J (Mus musculu

10 ngth variation between Mus musculus spp. and Mus spretus, and 32% showed variation between Mus muscul

11 wild mouse species, including Mus musculus, Mus spretus, and Mus spicelegus, as well as some inbred

12 o a second locus on proximal Chromosome 6 in Mus spretus, and this partial duplication was confirmed

13 length and ageing in mice, we have utilized Mus spretus as a model species because it has telomere l

14 other loci in three separate Mus musculus x Mus spretus backcross panels, we established the order o

15 mic DNAs from a (C57BL/6J x Mus spretus)F1 x Mus spretus backcross.

16 channel 4) to band F4 of the X chromosome in Mus spretus but to chromosome 7 in laboratory strains.

17 is X-linked and subject to X inactivation in Mus spretus, but that the same gene is autosomal in labo

18 The large Mus spretus/C57BL/6 backcross of 982 progeny has a genet

19 e performed RNA sequencing in Mus musculus x Mus spretus cells with complete skewing of X inactivatio

20 To determine if the polytropic proviruses of Mus spretus contain functional genes, we inoculated neon

21 Mus spretus diverged from Mus musculus over one million

22 o mouse species, Mus musculus domesticus and Mus spretus, drives chromosome decondensation and mis-se

23 1Mit4, using genomic DNAs from a (C57BL/6J x Mus spretus)F1 x M. spretus backcross.

24 1), by using genomic DNAs from a (C57BL/6J x Mus spretus)F1 x Mus spretus backcross.

25 c backcross panel from the cross (C57BL/6J x Mus spretus)F1 x Mus spretus probed with the mouse COX V

26 p16) and Cdkn2b(p15), and between BALB/c and Mus spretus for Cdkn2c(p18(INK4c)) were used to position

27 terspecific crosses between Mus musculus and Mus spretus for the detection of strong genetic interact

28 imprinting is investigated by introducing a Mus spretus H19 gene into heterologous locations in the

29 The mouse Mus spretus has been used to assess the biological respo

30 telomeres, although a related mouse species, Mus spretus, has human-sized telomeres.

31 susceptibility in interspecific Mus musculus/Mus spretus hybrid mice and have identified another seve

32 mouse strains, Mus musculus subspecies, and Mus spretus identified 29 ERVs of mouse mammary tumor vi

33 interspecific mouse crosses (Mus musculus x Mus spretus) identified the gene encoding Aurora2 (Stk6

34 rspecific backcross between Mus musculus and Mus spretus inbred strains.

35 everal wild mice (Mus dunni, SC-1 cells, and Mus spretus) mediated infections by both X-MLVs and P-ML

36 An interspecific backcross of SB/Le and Mus spretus mice was used to generate a molecular geneti

37 ts of an industrial settlement on inhabitant Mus spretus mice.

38 cells or xenomitochondrial cybrids harboring Mus spretus mtDNA.

39 Southern blot of C57BL/6J and Mus spretus murine genomic DNA with mY1 and mY3 gene-spe

40 ed to cytoplasts prepared from Mus musculus, Mus spretus, or rat (Rattus norvegicus), a comparable nu

41 ice using two mouse strains A/J (Par1/-) and Mus spretus (Par1/+).

42 from the cross (C57BL/6J x Mus spretus)F1 x Mus spretus probed with the mouse COX VIa-H cDNA.

43 rom 45 different strains of Mus musculus and Mus spretus revealed extensive polymorphism involving al

44 It has been reported elsewhere that Mus spretus SEG mice resist plague and develop an immune

45 Mice of the Mus spretus species are resistant to tumour development,

46 ween C57BL/6J (B6) and either C3H/HeJ (H) or Mus spretus (SPRET) occurred in four zones (A-D); zone A

47 omal clones) to map sequence variation among Mus spretus (SPRET/Ei and SPRET/Glasgow) and Mus musculu

48 Mus musculus (telomere length >25 kb) and Mus spretus (telomere length 5-15 kb) were used to gener

49 SPRET/Ei is an inbred strain derived from Mus spretus that has approximately 1% sequence differenc

50 In Mus spretus, the chloride channel 4 gene Clcn4-2 is X-li

51 [7] [9], the rat, and the wild mouse species Mus spretus, the gene is entirely X-unique.

52 musculus domesticus) and the Algerian mouse (Mus spretus), using samples from the ranges of sympatry

53 olymorphism in intron 2 between C57BL/6J and Mus spretus was used to map this gene to Chromosome 5 ne

54 hat are polymorphic between Mus musculus and Mus spretus, we used The Jackson Laboratory (TJL) inters

55 Notably, MeCP2 foci are absent in Mus spretus which is a mouse subspecies lacking methylat

56 g occurs in normal tissues of interspecific (Mus spretus x C57BL/6) mice.

57 of three independent Mus musculus NIH/Ola x (Mus spretus x M. musculus NIH/Ola)F1 backcrosses, to ide

58 a complete interspecific backcross [outbred Mus spretus X Mus musculus (NIH/Ola)].

59 ed by the backcross of (lean C57BL/6J x lean Mus spretus) x C57BL/6J, provides an excellent model of

60 [F1 female Spd/+ (female Spd/+ B6 x male +/+ Mus spretus) x male +/+ B6] exhibit highly variable cran